Canonical Allele Identifier: CA1620073568

Gene: BAK1 GGNBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.33575258_33575261delinsAGAG , CM000668.2:g.33575258_33575261delinsAGAG	GRCh38
NC_000006.11:g.33543035_33543038delinsAGAG , CM000668.1:g.33543035_33543038delinsAGAG	GRCh37
NC_000006.10:g.33651013_33651016delinsAGAG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374467.4:c.350+37_350+40delinsCTCT (BAK1) MANE Select	ENSP00000363591.3:n.350+37_350+40delinsCTCT
ENST00000360661.9:c.290+37_290+40delinsCTCT (BAK1)	ENSP00000353878.6:n.290+37_290+40delinsCTCT
ENST00000374467.3:c.350+37_350+40delinsCTCT (BAK1)	ENSP00000363591.3:n.350+37_350+40delinsCTCT
ENST00000442998.6:c.350+37_350+40delinsCTCT (BAK1)	ENSP00000391258.2:n.350+37_350+40delinsCTCT
ENST00000612409.1:n.249-93_249-90delinsAGAG (GGNBP1)
NM_001188.3:c.350+37_350+40delinsCTCT (BAK1)	NP_001179.1:n.350+37_350+40delinsCTCT
XM_011514779.1:c.350+37_350+40delinsCTCT (BAK1)	XP_011513081.1:n.350+37_350+40delinsCTCT
XM_011514780.1:c.173+37_173+40delinsCTCT (BAK1)	XP_011513082.1:n.173+37_173+40delinsCTCT
XM_011514779.3:c.350+37_350+40delinsCTCT (BAK1)	XP_011513081.1:n.350+37_350+40delinsCTCT
NM_001188.4:c.350+37_350+40delinsCTCT (BAK1) MANE Select	NP_001179.1:n.350+37_350+40delinsCTCT